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Synthesis and herbicidal activity of 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone derivatives.
J Agric Food Chem. 2009 Jan 28; 57(2):610-7.JA

Abstract

A series of novel 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone derivatives (3) were synthesized, and their structures including configuration of C=N bond were confirmed by (1)H NMR, elemental analysis and X-ray diffraction analysis. The bioassay showed that some of them exhibited excellent herbicidal activity against Amaranthus tricolor L. The activity of compounds 3 except compounds 3A1-2 was much higher than the commercial herbicide 2,4-D and the activity of about half of compounds 3 was comparable to the commercial herbicide tribenuron-methyl. The further bioassay showed that the representative of compounds 3, 3A1-12, exhibited excellent herbicidal activity not only against dicotyledon, such as Amaranthus tricolor L., Cucumis sativus L., Glycine max L., and Phaseolus radiatus L., but also against monocotyledon, such as Zea mays L. and Oryza sativa L.

Authors+Show Affiliations

Key Laboratory of Pesticide Chemistry and Application Technology, Department of Applied Chemistry, China Agricultural University, Beijing.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

19117417

Citation

Meng, Xiang-Qing, et al. "Synthesis and Herbicidal Activity of 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone Derivatives." Journal of Agricultural and Food Chemistry, vol. 57, no. 2, 2009, pp. 610-7.
Meng XQ, Zhang JJ, Liang XM, et al. Synthesis and herbicidal activity of 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone derivatives. J Agric Food Chem. 2009;57(2):610-7.
Meng, X. Q., Zhang, J. J., Liang, X. M., Zhu, W. J., Dong, Y. H., Wu, X. M., Huang, J. X., Rui, C. H., Fan, X. L., Chen, F. H., & Wang, D. Q. (2009). Synthesis and herbicidal activity of 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone derivatives. Journal of Agricultural and Food Chemistry, 57(2), 610-7. https://doi.org/10.1021/jf802649w
Meng XQ, et al. Synthesis and Herbicidal Activity of 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone Derivatives. J Agric Food Chem. 2009 Jan 28;57(2):610-7. PubMed PMID: 19117417.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Synthesis and herbicidal activity of 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone derivatives. AU - Meng,Xiang-Qing, AU - Zhang,Jian-Jun, AU - Liang,Xiao-Mei, AU - Zhu,Wei-Juan, AU - Dong,Yan-Hong, AU - Wu,Xue-Min, AU - Huang,Jia-Xing, AU - Rui,Chang-Hui, AU - Fan,Xian-Lin, AU - Chen,Fu-Heng, AU - Wang,Dao-Quan, PY - 2009/1/2/entrez PY - 2009/1/2/pubmed PY - 2009/2/14/medline SP - 610 EP - 7 JF - Journal of agricultural and food chemistry JO - J. Agric. Food Chem. VL - 57 IS - 2 N2 - A series of novel 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone derivatives (3) were synthesized, and their structures including configuration of C=N bond were confirmed by (1)H NMR, elemental analysis and X-ray diffraction analysis. The bioassay showed that some of them exhibited excellent herbicidal activity against Amaranthus tricolor L. The activity of compounds 3 except compounds 3A1-2 was much higher than the commercial herbicide 2,4-D and the activity of about half of compounds 3 was comparable to the commercial herbicide tribenuron-methyl. The further bioassay showed that the representative of compounds 3, 3A1-12, exhibited excellent herbicidal activity not only against dicotyledon, such as Amaranthus tricolor L., Cucumis sativus L., Glycine max L., and Phaseolus radiatus L., but also against monocotyledon, such as Zea mays L. and Oryza sativa L. SN - 1520-5118 UR - https://www.unboundmedicine.com/medline/citation/19117417/Synthesis_and_herbicidal_activity_of_12__aryloxyacyloxyimino__115_pentadecanlactone_derivatives_ L2 - https://dx.doi.org/10.1021/jf802649w DB - PRIME DP - Unbound Medicine ER -